# Schöpf–Schulz–Passarge syndrome

> SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy

**Wikidata**: [Q7433355](https://www.wikidata.org/wiki/Q7433355)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Schöpf–Schulz–Passarge_syndrome)  
**Source**: https://4ort.xyz/entity/sch-pf-schulz-passarge-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000135925/Orphanet_50944)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)